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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Mutism and CNTNAP2[original query]
A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits.
Biological psychiatry 2011 May 69 (9): 825-31.
Stein Murray B, Yang Bao-Zhu, Chavira Denise A, Hitchcock Carla A, Sung Sharon C, Shipon-Blum Elisa, Gelernter Jo
Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.
Psychiatric genetics 2012 Dec .
Toma C, Hervás A, Torrico B, Balmaña N, Salgado M, Maristany M, Vilella E, Martínez-Leal R, Planelles MI, Cuscó I, Del Campo M, Pérez-Jurado LA, Caballero-Andaluz R, de Diego-Otero Y, Pérez-Costillas L, Ramos-Quiroga JA, Ribasés M, Bayés M, Cormand B
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